Modified lipase and use thereof

ABSTRACT

The present invention addresses a problem of providing a lipase derived from a microorganism that is specific for short-chain to medium-chain fatty acids. A modified lipase is obtained by making a substitution in the amino acid sequence of a  Candida cylindracea  derived lipase, wherein the substitution is (1) a substitution of asparagine for an amino acid corresponding to the amino acid at position 428 in the amino acid sequence set forth in SEQ ID NO: 1; or (2) a substitution of phenylalanine, methionine, or isoleucine for an amino acid corresponding to the amino acid at position 429 in the amino acid sequence set forth in SEQ ID NO: 1.

TECHNICAL FIELD

The present invention relates to a modified lipase. Specifically, the present invention provides, for example, a modified lipase and a method for producing dairy products using such a modified lipase. The present application claims priority from Japanese Patent Application No. 2013-255419, filed on Dec. 10, 2013, the entire content of which is incorporated by reference.

BACKGROUND ART

Lipases have been used for formation and enhancement of the flavor of dairy products. Traditionally, there have been used preparations of lipases from kids, calves, or lambs. These ruminant lipases have a specificity that short-chain fatty acids (C₄ and C₆ fatty acids) are released from milk fat, and are suitable for the formation of the flavor of dairy products.

However, there is a strong industrial need for an alternative to animal-derived lipases because kosher or halal qualities are required for enzyme preparations utilized for food processing. To meet the need, proposals have been made, for example, to use microbial enzymes (for example, Patent Document 1) and recombinant enzymes (for example, Patent Document 2). In addition, attempts have also been made to modify lipases by genetic engineering, for application to particular purposes (for example, Patent Documents 3 to 5).

CITATIONS LIST Patent Literatures

Patent Literature 1: JP 61-135541 A

Patent Literature 2: US 2004/0001819

Patent Literature 3: JP 2011-512809

Patent Literature 4: JP 2003-524386

Patent Literature 5: JP 2004-517639

Non Patent Literature

Non Patent Literature 1: J. Schmitt et al., Protein Engineering, vol. 15, no. 7, pp. 595-601, 2002

SUMMARY OF INVENTION Technical Problems

Microbial lipases are more specific for long-chain fatty acids than for short-chain fatty acids, and thus their action on milk fat will give a profile that many of the fatty acids released from the milk fat have a long chain. Long-chain fatty acids, which are responsible for soap odor, are not favorable as the favor of dairy products, particularly of cheeses.

Under this background, the present invention addresses a problem of providing a lipase derived from a microorganism that is specific for short-chain to medium-chain fatty acids, and a use of such a lipase.

Solutions to Problems

In the course of the investigation to solve the above-mentioned problem, the inventors focused on a Candida cylindracea derived lipase (a lipase formerly referred to as a Candida rugosa derived lipase was used) and attempted its modification. After trial and error, the inventors succeeded in finding very useful mutation sites that can lead to the achievement of the goals of the present invention, from the amino acids which form the substrate pocket. Variants with a given amino acid substitution made at each of these mutation sites hydrolyzed milk fat so that short-chain to medium-chain fatty acids (C₄ to C₈ fatty acids) were selectively released as in the case of an animal lipase. These variants worked well on short-chain fatty acids (C₄ to C₆ fatty acids), and best on C₄ fatty acid. As just mentioned, the inventors succeeded, as a result of these amino acid mutations, in bringing the substrate specificities of lipases close to that of the animal lipase. In connection with this, for the Candida cylindracea derived lipase, there have been reported mutations (amino acid substitutions) considered to be effective for its substrate specificity (Non-Patent Document 1), but it was observed that the newly found mutations were more effective in modifying the substrate specificity (specificity for short-chain fatty acids).

In present invention, it is likely that mutagenesis procedures similar to those as described herein can also be applied to other enzymes having a high degree of amino acid sequence identity relative to LIP1 used in Examples, in light of common general technical knowledge that enzymes having a high degree of amino acid sequence identity (typically isozymes) have a high degree of similarity in their three-dimensional structure, particularly in sites involved in their activity, such as active site and substrate pocket, and that it is highly probable that a similar mutation in such enzymes gives rise to a similar effect.

The inventions described below are based mainly on the above-described results and observation.

[1] A modified lipase consisting of an amino acid sequence with a substitution made in the amino acid sequence of a Candida cylindracea derived lipase, wherein the substitution is:

(1) a substitution of asparagine for an amino acid corresponding to the amino acid at position 428 in the amino acid sequence set forth in SEQ ID NO: 1; or

(2) a substitution of phenylalanine, methionine, or isoleucine for an amino acid corresponding to the amino acid at position 429 in the amino acid sequence set forth in SEQ ID NO: 1.

[2] The modified lipase according to [1], wherein the amino acid sequence of the Candida cylindracea derived lipase is an amino acid sequence that is 70% or more identical to the amino acid sequence of SEQ ID NO: 2 and wherein the substitution is the substitution represented in (1).

[3] The modified lipase according to [1], wherein the amino acid sequence of the Candida cylindracea derived lipase is an amino acid sequence that is 90% or more identical to the amino acid sequence of SEQ ID NO: 2 and wherein the substitution is the substitution represented in (2).

[4] The modified lipase according to [2] or [3], wherein the amino acid sequence of the Candida cylindracea derived lipase is an amino acid sequence of any one of SEQ ID NOs: 2 to 7.

[5] The modified lipase according to [1], consisting of the amino sequence set forth in any one of SEQ ID NOs: 8 to 11.

[6] A gene encoding the modified lipase according to any one of [1] to [5].

[7] The gene according to [6], comprising the base sequence set forth in any one of SEQ ID NOs: 12 to 19.

[8] A recombinant DNA comprising the gene according to [6] or [7].

[9] A microorganism carrying the recombinant DNA according to [8].

[10] The microorganism according to [9], wherein the host is Escherichia coli, Candida cylindracea, Aspergillus oryzae, Bacillus subtilis, or Pichia pastoris.

[11] An enzyme preparation comprising the modified lipase according to any one of [1] to [5].

[12] A method for improving the flavor of a food product or food raw material, characterized in that the enzyme according to any one of [1] to [5] or the enzyme preparation according to [11] is allowed to act on the food product or food raw material.

[13] A method for producing a food product, characterized in that the enzyme according to any one of [1] to [5] or the enzyme preparation according to [11] is allowed to act on a food raw material or intermediate product.

[14] The method according to [12] or [13], wherein the food product is a dairy product.

[15] A flavor-improving agent that is allowed to act on a food product or food raw material, comprising the enzyme according to any one of [1] to [5] or the enzyme preparation according to [11].

[16] A food product or food raw material obtained by treatment with the enzyme according to any one of [1] to [5] or the enzyme preparation according to [11].

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows the composition of released fatty acids after treatment with a wild-type enzyme. A Candida cylindracea derived wild-type lipase LIP1 was allowed to act on cheese (used as a substrate) and the composition of the released fatty acids was analyzed.

FIG. 2 shows the composition of released fatty acids after treatment with modified enzymes. Various modified lipases (variants) were allowed to act on cheese (used as a substrate) and a comparison was made for the compositions of the released fatty acids. The upper left panel shows results when a calf sublingual gland derived lipase was used. The lower panels show results when modified lipases were used (variant 1: L428N; variant 2: G429F, variant 3: G429M; and variant 4: G429I). The upper right panel shows results when a modified lipase (L428F) that had previously been reported was used.

FIG. 3 shows a comparison of the sequences of Candida cylindracea derived wild-type lipases LIP1 (SEQ ID NO: 2), LIP1′ (SEQ ID NO: 3), LIP2 (SEQ ID NO: 4), LIPS (SEQ ID NO: 5), LIP4 (SEQ ID NO: 6), and LIPS (SEQ ID NO: 7).

FIG. 4 is a continuation of FIG. 3.

FIG. 5 is a continuation of FIG. 4.

DESCRIPTION OF EMBODIMENTS

For convenience of description, some of the terms used in relation to the present invention are defined as follows.

(Terminology)

The term “modified lipase” refers to an enzyme obtained by modification or mutation of a particular lipase (which is referred to as a “reference lipase” for convenience of description). The reference lipase is a Candida cylindracea derived lipase or a Candida rugosa derived lipase. The terms “Candida cylindracea derived lipase” and “Candida rugosa derived lipase” are used interchangeably.

The term “Candida cylindracea derived lipase” is a lipase that is obtained from a strain of Candida cylindracea as the source, and includes lipases produced by Candida cylindracea, lipases produced by mutated strains of Candida cylindracea (variant strains), lipases expressed, for example, in other microorganism, using the genetic information of such enzymes, or the like. Similarly, the term “Candida rugosa derived lipase” is a lipase that is obtained from a strain of Candida rugosa as the source, and includes lipases produced by Candida rugosa, lipases produced by mutated strains of Candida rugosa (variant strains), lipases expressed, for example, in other microorganism, using the genetic information of such enzymes, or the like.

In the present invention, an “amino acid substitution” is carried out as modification or mutation. Therefore, some amino acid residues are found to be different when a modified lipase and the reference lipase therefor are compared. In the specification, a modified lipase is also referred to as a modified enzyme or as a variant.

In the specification, amino acids are designated according to the common practice, as their single letters as described below:

methionine: M; serine: S; alanine: A; threonine: T; valine: V; tyrosine: Y; leucine: L; asparagine: N; isoleucine: I; glutamine: Q; proline: P; aspartic acid: D; phenylalanine: F; glutamic acid: E; tryptophan: W; lysine: K; cysteine: C; arginine: R; glycine: G; and histidine: H.

In the specification, the positions of amino acids in an amino acid sequence are specified by assigning the numbers from the N-terminus toward the C-terminus of the amino acid sequence, wherein according to customary practice, the methionine corresponding to the translation initiation site is assigned to 1, i.e., the first amino acid. Therefore, in the case of the sequence of a mature protein in which the signal peptide has been removed, the amino acid numbers are decreased by the number of the amino acids of the signal peptide.

In the specification, an amino acid residue at a mutation site (an amino acid residue to be substituted with another amino acid) is expressed in a combination of the above-described single letter representing the kind of the amino acid residue and the figure representing the position of the amino acid residue. For example, if proline at position 428 is a mutation site, then the amino acid is designated as “G428.”

1. Modified lipases

A first aspect of the present invention is directed to a modified lipase (modified enzyme). The modified enzyme of the present invention has an amino acid sequence with a substitution made in the amino acid sequence of a Candida cylindracea derived lipase, wherein the substitution is:

(1) a substitution of asparagine for an amino acid corresponding to the amino acid at position 428 in the amino acid sequence set forth in SEQ ID NO: 1; or

(2) a substitution of phenylalanine, methionine, or isoleucine for an amino acid corresponding to the amino acid at position 429 in the amino acid sequence set forth in SEQ ID NO: 1.

The sequence of SEQ ID NO: 1 is the amino acid sequence of a Candida cylindracea derived lipase LIP 1, which comprises the signal peptide. In the substitution represented in (1), an amino acid corresponding to the amino acid at position 428 in this amino acid sequence is a target to be substituted with a given amino acid and is substituted with asparagine, resulting in an alteration of the substrate specificity of the lipase. In the substitution represented in (2), an amino acid corresponding to the amino acid at position 429 in the sequence of SEQ ID NO: 1 is a target to be substituted with a given amino acid and is substituted with phenylalanine, methionine, or isoleucine, resulting in an alteration of the substrate specificity of the lipase. Lipases after these amino acid substitutions, i.e., modified enzymes have an increased specificity for short-chain to medium-chain fatty acids (C₄ to C₈ fatty acids), and when allowed to act on milk fat, typically give a composition of the released fatty acids that is similar to that of a calf sublingual gland derived lipase. Preferably, these modified enzymes work well on short-chain fatty acids (C₄ to C₆ fatty acids), and best on C₄ fatty acid.

Herein, the term “corresponding” when used for an amino acid residue in the present specification means contributing equally to exhibition of functions among proteins (enzymes)being compared. For example, when an amino acid sequence for comparison to the base amino acid sequence (that is, the amino acid sequence set forth in SEQ ID NO: 1) is aligned while considering partial homology of the primary structure (that is, an amino acid sequence) so that the most appropriate comparison can be achieved (in this event, the alignment may be optimized by introducing gaps if necessary), an amino acid located at a position corresponding to a specific amino acid in the base amino acid sequence can be specified as a “corresponding amino acid”. The “corresponding amino acid” can also be specified by comparison between conformations (three-dimensional structures) in place of or in addition to the comparison between primary structures. Utilization of conformational information can give highly credible comparison results. In this case, a technique of performing an alignment with comparing atomic coordinates of conformations of a plurality of enzymes can be adopted. Conformational information of an enzyme to be mutated is available from, for example, the Protein Data Bank (http://www.pdbj.org/indexj.html).

One example of a method for determination of a protein conformation by the X-ray crystal structure analysis will be shown below.

(1) A protein is crystallized. Crystallization is essential to determine a conformation, and in addition, crystallization is industrially useful as a purification method of a protein at high purity and a stable preservation method of a protein at high density. In this case, a protein to which a substrate as a ligand or its analogous compound is bound may be preferably used for crystallization.

(2) The prepared crystal is irradiated with X ray to collect diffraction data. There are many cases that a protein crystal is damaged due to X ray irradiation and the diffraction ability is deteriorated. In such cases, a low-temperature measurement technique of rapidly cooling the crystal to about −173° C. and collecting diffraction data in the state has been recently prevailed. In addition, ultimately, synchrotron orbit radiation having high luminance is utilized to collect high resolution data that is used for structural determination.

(3) In addition to the diffraction data, phase information is necessary in order to perform the crystal structure analysis. When a crystal structure of an analogous protein to a desired protein is unknown, it is impossible to determine the structure in a molecular substitution method, and a phase problem has to be solved by a heavy-atom isomorphous replacement method. The heavy-atom isomorphous replacement method is a method in which a metallic atom having a high atomic number such as mercury or platinum is introduced into a crystal and contribution of a large X ray scattering ability of such a metallic atom to X ray diffraction data is utilized to collect phase information. The determined phase is possibly improved by smoothing an electron density of a solvent region in the crystal. Since a water molecule in the solvent region has large fluctuation, the electron density is hardly observed, and thus adjusting the electron density in this region to close to 0 makes it possible to approach the real electron density, which results in improving a phase. When plural molecules are contained in an asymmetrical unit, equation of electron densities of these molecules makes it possible to more significantly improve a phase. A model of a protein is fit to an electron density map calculated using the phase improved as described above. This process is performed on computer graphics using a program such as QUANTA made by MSI Co. (USA). After the process, structural precision is performed using a program such as X-PLOR made by MSI Co. to complete the structure analysis. When a crystal structure of an analogous protein to a desired protein is known, it can be determined in a molecular substitution method using the atomic coordinate of the known protein. Molecular substitution and structure refinement can be performed using a program such as CNS_SOLVE ver.11.

As Candida cylindracea derived lipases, there are known five enzymes (LIP1, LIP2, LIPS, LIP4, and LIP5). In addition, the applicant has found an enzyme (referred to as LIP1′) that exhibits a high homology to LIP1, from lipase-producing mutant strains. For these six enzymes, the amino acid sequences without the signal peptide, i.e., the amino acid sequences of the mature enzymes are set forth in SEQ ID NOs: 2 (for LIP1), 3 (for LIP1′), 4 (for LIP2), 5 (for LIP3), 6 (for LIP4), and 7 (for LIP5). Typically, one of these enzymes will be used as a reference lipase (which is subjected to amino acids substitutions, resulting in the generation of modified enzymes). Therefore, specific examples of the amino acid sequence of a reference lipase are the amino acid sequences of SEQ ID NOs: 2 to 7. The identity to the amino acid sequence of Candida cylindracea derived lipase LIP1 (SEQ ID NO: 2) is 99% for the amino acid sequence of SEQ ID NO: 3, 79% for the amino acid sequence of SEQ ID NO: 4, 88% for the amino acid sequence of SEQ ID NO: 5, 81% for the amino acid sequence of SEQ ID NO: 6, and 82% for the amino acid sequence of SEQ ID NO: 7 (FIGS. 3 to 5).

For the substitution represented in (1) (a substitution for an amino acid corresponding to the amino acid at position 428 in the amino acid sequence of SEQ ID NO: 1), an enzyme consisting of an amino acid sequence 70% or more identical to the amino acid sequence of SEQ ID NO: 2 may be used as a reference lipase. For example, any of LIP1, LIP1′, LIP2, LIP3, LIP4, and LIP5 can be the reference lipase. As a reference lipase, use is preferably made of an enzyme that has an amino acid sequence having 80% or more identity to the amino acid sequence of SEQ ID NO: 2 (with the proviso that the enzyme exhibits lipase activity), more preferably an enzyme that has an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 2 (with the proviso that the enzyme exhibits lipase activity), even more preferably an enzyme that has an amino acid sequence having 95% or more identity to the amino acid sequence of SEQ ID NO: 2 (with the proviso that the enzyme exhibits lipase activity), and most preferably an enzyme that has an amino acid sequence having 99% or more identity to the amino acid sequence of SEQ ID NO: 2 (with the proviso that the enzyme exhibits lipase activity).

In LIP1 having the amino acid sequence of SEQ ID NO: 2, the amino acid corresponding to the amino acid at position 428 in the amino acid sequence of SEQ ID NO: 1 is leucine (L) at position 413. Therefore, when LIP1 having the amino acid sequence of SEQ ID NO: 2 is used as a reference lipase, this amino acid is a target to be substituted with a given amino acid. On the other hand, when LIP1′ having the amino acid sequence of SEQ ID NO: 3 is used as a reference lipase, the amino acid to be substituted with a given amino acid is leucine (L) that is an amino acid located at position 413 in SEQ ID NO: 3. When LIP2 having the amino acid sequence of SEQ ID NO: 4 is used as a reference lipase, the amino acid to be substituted with a given amino acid is leucine (L) that is an amino acid located at position 413 in the amino acid sequence of SEQ ID NO: 4. When LIP3 having the amino acid sequence of SEQ ID NO: 5 is used as a reference lipase, the amino acid to be substituted with a given amino acid is leucine (L) that is an amino acid located at position 413 in SEQ ID NO: 5. When LIP4 having the amino acid sequence of SEQ ID NO: 6 is used as a reference lipase, the amino acid to be substituted with a given amino acid is leucine (L) that is an amino acid located at position 413 in the amino acid sequence of SEQ ID NO: 6. When LIPS having the amino acid sequence of SEQ ID NO: 7 is used as a reference lipase, the amino acid to be substituted with a given amino acid is leucine (L) that is an amino acid located at position 413 in the amino acid sequence of SEQ ID NO: 7.

In the meanwhile, for the substitution represented in (2) (a substitution for an amino acid corresponding to the amino acid at position 429 in the amino acid sequence of SEQ ID NO: 1), an enzyme consisting of an amino acid sequence 90% or more identical to the amino acid sequence of SEQ ID NO: 2 may be used as a reference lipase. For example, any of LIP1 and LIP1′ can be the reference lipase. As a reference lipase, use is preferably made of an enzyme that has an amino acid sequence having 95% or more identity to the amino acid sequence of SEQ ID NO: 2 (with the proviso that the enzyme exhibits lipase activity), more preferably an enzyme that has an amino acid sequence having 98% or more identity to the amino acid sequence of SEQ ID NO: 2 (with the proviso that the enzyme exhibits lipase activity), and most preferably an enzyme that has an amino acid sequence having 99% or more identity to the amino acid sequence of SEQ ID NO: 2 (with the proviso that the enzyme exhibits lipase activity).

In LIP1 having the amino acid sequence of SEQ ID NO: 2, the amino acid corresponding to the amino acid at position 429 in the amino acid sequence of SEQ ID NO: 1 is glycine (G) at position 414. Therefore, when LIP1 having the amino acid sequence of SEQ ID NO: 2 is used as a reference lipase, this amino acid is a target to be substituted with a given amino acid. On the other hand, when LIP 1′ having the amino acid sequence of SEQ ID NO: 3 is used as a reference lipase, the amino acid to be substituted with a given amino acid is glycine (G) that is an amino acid located at position 414 in SEQ ID NO: 3.

Here, specific examples of the amino acid sequences of modified enzymes are represented in SEQ ID NOs: 8 to 11. A modified enzyme having the amino acid sequence of SEQ ID NO: 8 (variant 1) is obtained by making a substitution of asparagine for an amino acid at position 413 on LIP1 having the amino acid sequence of SEQ ID NO: 2 (that is, a substitution represented in (1)); a modified enzyme having the amino acid sequence of SEQ ID NO: 9 (variant 2) is obtained by making a substitution of phenylalanine for an amino acid at position 414 on LIP1 having the amino acid sequence of SEQ ID NO: 2 (that is, one of the substitution represented in (2)); a modified enzyme having the amino acid sequence of SEQ ID NO: 10 (variant 3) is obtained by making a substitution of methionine for an amino acid at position 414 on LIP1 having the amino acid sequence of SEQ ID NO: 2 (that is, one of the substitution represented in (2)); and a modified enzyme having the amino acid sequence of SEQ ID NO: 11 (variant 4) is obtained by making a substitution of isoleucine for an amino acid at position 414 on LIP1 having the amino acid sequence of SEQ ID NO: 2 (that is, one of the substitution represented in (2)).

In cases where a portion of the amino acid sequence of a given protein has been subjected to mutagenesis, a mutated version of the protein may have a function equivalent to the original unmutated protein. That is, it is sometimes observed that a mutation in a given amino acid sequence does not lead to substantial effects on the function of the protein, which is maintained between before and after introducing the mutation. Taking this common general technical knowledge into account, it can be considered that when compared to an above-described modified enzyme (any of variants 1 to 4), a modified enzyme which has a slight difference in the amino acid sequence (wherein the difference in the amino acid sequence is located at a position(s) other than the position at which the above-described amino acid substitution has been performed), but which nevertheless does not have substantial differences in properties is an enzyme that is substantially the same as the above-described modified enzyme. The “slight difference in the amino acid sequence” in this context typically refers to the occurrence of a mutation(s) (change(s)) in the amino acid sequence resulting from deletion or substitution of one to several amino acids (for example, up to three, five, seven, or ten amino acids) contained in the amino acid sequence, or addition or insertion of one to several amino acids (for example, up to three, five, seven, or ten amino acids), or combinations thereof. The identity (%) between the amino acid sequences of “an enzyme that is substantially the same” and an above-described modified enzyme that is used as the reference is, for example, 90% or more, preferably 95% or more, more preferably 98% or more, most preferably 99% or more. Differences in the amino acid sequence may occur at more than one position. A “slight difference in the amino acid sequence” preferably results from conservative amino acid substitution.

2. Nucleic acid coding for modified lipase, etc.)

The second aspect of the present invention provides a nucleic acid relating to the modified enzyme of the invention. That is, provided are a gene coding for the modified enzyme, a nucleic acid that can be used as a probe for identifying a nucleic acid coding for the modified enzyme, and a nucleic acid that can be used as a primer for amplifying or mutating a nucleic acid coding for the modified enzyme.

The gene coding for a modified enzyme is typically used in preparation of the modified enzyme. According to a genetic engineering procedure using the gene coding for a modified enzyme, a modified enzyme in a more homogeneous state can be obtained. Further, the method can be a preferable method also in the case of preparing a large amount of a modified enzyme. Note that uses of the gene coding for a modified enzyme are not limited to preparation of a modified enzyme. For example, the nucleic acid can also be used as a tool for an experiment intended for clarification of action mechanisms of a modified enzyme or a tool for designing or preparing a further modified form of an enzyme.

The “gene coding for a modified enzyme” herein refers to a nucleic acid capable of obtaining the modified enzyme when it is expressed, and includes, as a matter of course of a nucleic acid having a base sequence corresponding to the amino acid sequence of the modified enzyme, also a nucleic acid obtained by adding a sequence that does not code for an amino acid sequence to such a nucleic acid. Degeneracy of a codon is also considered.

Examples of the (base) sequence of the gene encoding a modified enzyme are represented in SEQ ID NOs: 12 to 15. These sequences encode variants described in the Examples section which follows, as indicated below.

SEQ ID NO: 12: variant 1 (L428N)

SEQ ID NO: 13: variant 2 (G429F)

SEQ ID NO: 14: variant 3 (G429M)

SEQ ID NO: 15: variant 4 (G429I)

In Candida cylindracea, the CTG codon encodes serine. If a gene is recombinantly expressed using other yeasts and the like as a host, then it is necessary that depending on the host to be used, the CTG codon is changed to another codon encoding serine (TCT, TCC, TCA, ATG, or AGC). The present invention also provides, as the sequence of a gene for use in heterologous expression, a sequence in which a codon substitution of this type is made for the sequence of any one of SEQ ID NOs: 12 to 15. Examples of sequences with a codon substitution are as follows.

SEQ ID NO: 16, which is a sequence with a codon substitution in the sequence of SEQ ID NO: 12;

SEQ ID NO: 17, which is a sequence with a codon substitution in the sequence of SEQ ID NO: 13;

SEQ ID NO: 18, which is a sequence with a codon substitution in the sequence of SEQ ID NO: 14; and

SEQ ID NO: 19, which is a sequence with a codon substitution in the sequence of SEQ ID NO: 15.

When a gene according to the present invention is to be expressed in a host, the gene will usually be inserted into the host in the form of a gene construct in which the above-described sequence has a signal peptide-coding sequence (a signal sequence) added thereto at the 5′ end. The signal sequence of wild-type LIP1 is represented in SEQ ID NO: 21. The amino acid sequence encoded by this signal sequence (that is, the signal peptide) is represented in SEQ ID NO: 22. The signal sequence may be selected depending on the host to be used. Any signal sequence that can express a variant of interest can be used in the present invention. Examples of the signal sequence that can be used in the present invention can be illustrated by the following: a sequence encoding the signal peptide of the α-factor (Protein Engineering, 1996, vol. 9, p. 1055-1061), a sequence encoding the signal peptide of the α-factor receptor, a sequence encoding the signal peptide of the SUC2 protein, a sequence encoding the signal peptide of the PHOS protein, a sequence encoding the signal peptide of the BGL2 protein, a sequence encoding the signal peptide of the AGA2 protein, a sequence encoding the signal peptide of TorA (trimethylamine N-oxidoreductase), a sequence encoding the signal peptide of Bacillus subtilis derived PhoD (phosphoesterase), a sequence encoding the signal peptide of Bacillus subtilis derived LipA (lipase), a sequence encoding the signal peptide of Aspergillus oryzae derived Taka-amylase (JP 2009-60804 A), a sequence encoding the signal peptide of Bacillus amyloliquefaciens derived α-amylase (Eur. J. Biochem. 155, 577-581 (1986)), a sequence encoding the signal peptide of Bacillus subtilis derived neutral protease (APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Apr. 1995, p. 1610-1613, Vol. 61, No. 4), and a sequence encoding the signal peptide of Bacillus derived cellulase (JP 2007-130012 A).

The nucleic acid of the present invention can be prepared in an isolated state by use of a standard genetic engineering technique, molecular biological technique, biochemical technique, and the like in reference to the present specification or the sequence information disclosed in the appended sequence listing.

Another embodiment of the present invention provides a nucleic acid different in a base sequence in a part (hereinafter also referred to as a “homologous nucleic acid”, and a base sequence defining a homologous nucleic acid is also referred to as a “homologous base sequence”) as compared to the base sequence of the gene coding for the modified enzyme of the invention, although functions of a protein coded by the nucleic acid are equal. An example of the homologous nucleic acid includes a DNA composed of a base sequence containing substitution, deletion, insertion, addition or inversion of 1 to several bases on the basis of the base sequence of the nucleic acid coding for the modified enzyme of the present invention and coding for a protein having activity which is characteristic to the modified enzyme (i.e. lipase activity). Substitution or deletion of bases may occur in a plurality of sites. The “plurality” herein depends on positions or kinds of amino acid residues in a conformation of a protein coded by the nucleic acid but means, for example, 2 to 40 bases, preferably 2 to 20 bases, and more preferably 2 to 10 bases.

Such a homologous nucleic acid as described above can be obtained by, for example, a restriction enzyme treatment, a treatment with exonuclease, DNA ligase, etc., and introduction of mutation by a site directed mutation introduction method (Molecular Cloning, Third Edition, Chapter 13, Cold Spring Harbor Laboratory Press, New York), and random mutation introduction method (Molecular Cloning, Third Edition, Chapter 13, Cold Spring Harbor Laboratory Press, New York). The homologous nucleic acid can be obtained also in other methods such as exposure to ultraviolet radiation.

Another embodiment of the present invention relates to a nucleic acid having a base sequence complementary to the base sequence of the gene coding for the modified enzyme of the invention. Another embodiment of the present invention provides a nucleic acid having a base sequence with an identity of at least about 60%, 70%, 80%, 90%, 95%, 99%, or 99.9% to the base sequence of the gene coding for the modified enzyme of the invention or a base sequence complementary to the base sequence.

Another embodiment of the present invention relates to a nucleic acid having a base sequence hybridizing to a base sequence complementary to the base sequence of the gene coding for the modified enzyme of the invention or its homologous base sequence under stringent conditions. The “stringent conditions” herein refer to conditions wherein a so-called specific hybrid is formed and a nonspecific hybrid is not formed. Such stringent conditions are known by a person skilled in the art and can be set in reference to, for example, Molecular Cloning (Third Edition, Cold Spring Harbor Laboratory Press, New York) and Current protocols in molecular biology (edited by Frederick M. Ausubel et al., 1987). Examples of the stringent conditions include conditions of using a hybridization liquid (50% formamide, 10× SSC (0.15 M NaCl, 15 mM sodium citrate, pH 7.0), a 5× Denhardt solution, 1% SDS, 10% dextran sulfate, 10 μg/ml of modified salmon sperm DNA, and a 50 mM phosphate buffer (pH7.5)) and incubating at about 42° C. to about 50° C., thereafter washing with 0.1× SSC and 0.1% SDS at about 65° C. to about 70° C. Examples of more preferable stringent conditions include conditions of using 50% formamide, 5× SSC (0.15 M NaCl, 15 mM sodium citrate, pH 7.0), a 1× Denhardt solution, 1% SDS, 10% dextran sulfate, 10 μg/ml of modified salmon sperm DNA, and a 50 mM phosphate buffer (pH 7.5) as a hybridization liquid.

Another embodiment of the present invention provides a nucleic acid (nucleic acid fragment) having a part of the base sequence of the gene coding for the modified enzyme of the invention or a base sequence complementary to the base sequence. Such a nucleic acid fragment can be used in detection, identification, and/or amplification of a nucleic acid having the base sequence of the gene coding for the modified enzyme of the present invention. For example, the nucleic acid fragment is designed so as to at least contain a part being hybridized to a sequential nucleotide moiety (for example, about 10 to about 100 bases length, preferably about 20 to about 100 bases length, more preferably about 30 to about 100 bases length) in the base sequence of the gene coding for the modified enzyme of the invention. When used as a probe, the nucleic acid fragment can be labeled. Examples such as fluorescent substances, enzymes, and radioactive isotopes can be used for the labeling.

Another aspect of the present invention relates to a recombinant DNA containing the gene of the present invention (the gene coding for a modified enzyme). The recombinant DNA of the invention is provided in, for example, a form of a vector. The term “vector” in the present specification refers to a nucleic acid molecule that can transfer a nucleic acid inserted in the vector to a target such as a cell.

A suitable vector is selected according to its intended use (cloning, expression of a protein) and in consideration of a kind of a host cell. Examples include a M13 phage or an altered form thereof, a λ phage or an altered form thereof, and pBR322 or an altered form thereof (e.g., pB325, pAT153, pUC8), etc. as a vector having Escherichia coli as a host, pYepSecl, pMFa, and pYES2 as a vector having a yeast as a host, pAc, pVL, etc. as a vector having an insect cell as a host, and pCDM8, pMT2PC, etc. as a vector having a mammal cell as a host.

The vector of the present invention is preferably an expression vector. The “expression vector” refers to a vector capable of introducing a nucleic acid inserted in the expression vector into a target cell (host cell) and expressing it in the cell. The expression vector generally contains a promoter sequence necessary for expression of a nucleic acid inserted, an enhancer sequence for promoting expression, and the like. An expression vector containing a selective marker can also be used. When such an expression vector is used, presence or absence (and its degree) of introduction of the expression vector can be confirmed using a selective marker.

Insertion of the nucleic acid of the present invention into the vector, insertion of a selective marker gene (if necessary), insertion of a promoter (if necessary), and the like can be performed in a standard recombinant DNA technique (for example, a known method of using a restriction enzyme and a DNA ligase, which can be referred in Molecular Cloning, Third Edition, 1.84, Cold Spring Harbor Laboratory Press, New York).

As host cells, there can be employed, for example, microbial cells of koji mold

(for example, Aspergillus oryzae), bacilli (for example, Bacillus subtilis), Escherichia coli, and Saccharomyces cerevisiae, in terms of easy handling; however, any host cell in which a recombinant DNA can be replicated and a gene encoding a modified enzyme can be expressed can be utilized. Preferably, Escherichia coli and Saccharomyces cerevisiae can be employed as a host organism. Candida yeasts such as Candida cylindracea can also be used as a host organism. In addition, Pichia yeasts such as Pichia pastoris can also be used as a host organism. Strains of Escherichia coli can be Escherichia coli strain BL21(DE3)pLysS in cases of using a T7-based promoter, and Escherichia coli strain JM109 in other cases. Strains of Saccharomyces cerevisiae can be Saccharomyces cerevisiae strain SHY2, AH22, or INVSc1 (Invitrogen).

Another aspect of the present invention relates to a microorganism having the recombinant DNA of the invention (that is, a transformant). The microorganism of the invention can be obtained by transfection or transformation using the vector of the invention described above. The transfection or transformation can be performed in, for example, the calcium chloride method (J. Mol. Biol., 53, 159 (1970)), the Hanahan method (J. Mol. Biol., 166, 557 (1983)), the SEM method (Gene, 96, 23 (1990)), a method by Chung, et al. (Proc. Natl. Acad. Sci. U.S.A. 86, 2172 (1989)), the calcium phosphate coprecipitation method, electroporation (Potter, H. et al., Proc. Natl. Acad. Sci. U.S.A. 81, 7161-7165 (1984)), and lipofectin (Feigner, P. L. et al., Proc. Natl. Acad. Sci. U.S.A. 84, 7413-7417 (1984)). The microorganism of the present invention can be used for producing the modified enzyme of the invention.

3. Enzyme preparetion containing modified lipase

The modified enzyme of the present invention is provided, for example, in the form of an enzyme preparetion. The enzyme preparetion may contain an excipient, a buffer agent, a suspending agent, a stabilizer, a preservative, an antiseptic, saline and the like besides the active ingredient (the modified enzyme of the present invention). As the excipient, starch, dextrin, maltose, trehalose, lactose, D-glucose, sorbitol, D-mannitol, white soft sugar, glycerol and the like can be used. As the buffer agent, phosphates, citrates, acetates and the like can be used. As the stabilizer, propylene glycol, ascorbic acid and the like can be used. As the preservative, phenol, benzalkonium chloride, benzyl alcohol, chlorobutanol, methylparaben and the like can be used. As the antiseptic, ethanol, benzalkonium chloride, paraoxybenzoic acid, chlorobutanol and the like can be used.

4. Uses of modified lipases

A further aspect of the present invention is directed to uses of modified enzymes and enzyme preparations. A modified enzyme according to the present invention has a substrate specificity similar to that of an animal lipase, that is, a selectivity for short-chain to medium-chain fatty acids. Taking advantage of this property, the present invention utilizes such a modified enzyme or a preparation thereof for flavor improvement of food products or food raw materials. “Flavor improvement” refers to providing a given product or raw material with a more favorable flavor than its original flavor (that is, the flavor of the given product or raw material to which the present invention is not applied) by increasing or adding its particular flavor component(s). Typically, flavor improvement results in the enhancement of a flavor characteristic of a given food product or food raw material. The flavor may be improved by masking an unfavorable flavor component(s).

Food products or food raw materials to which the present invention can be applied can be illustrated by the following: dairy products, margarine-based products (margarines, fat spreads), shortenings, ice cream-based products (ice creams, gelati, frozen yogurts, sundaes, smoothies, soft creams, etc.), ices, mousses, Bavarian creams, snacks, dressings, soups, various vegetable oils (soybean oil, rapeseed oil, corn oil, palm oil, palm kernel oil, coconut oil, sunflower oil, cottonseed oil, etc.).

For example, by allowing a modified enzyme or enzyme preparation of the present invention to act on a food product or food raw material, its flavor can be improved. On the other hand, if a modified enzyme or enzyme preparation of the present invention is added to or mixed to a raw material or intermediate product in a step for producing the food product, then a food product with an improved flavor can be produced. Alternatively, the flavor of a food product or food raw material may be improved, for example, by addition or mixing of a composition that is obtained using a modified enzyme or enzyme preparation of the present invention.

A modified enzyme or enzyme preparation of the present invention is suitable particularly for the production of dairy products. The flavor of dairy products, particularly the cheese flavor, can be increased or improved by applying to them a modified enzyme or enzyme preparation of the present invention.

Examples of dairy products to which a modified enzyme or enzyme preparation of the present invention can be applied can include various types of cheese (Cheshire cheese, Cheddar cheese, Edam cheese, Gouda cheese, Emmental cheese, Parmesan cheese, Pecorino cheese, etc.), processed cheese (process cheese), EMC (Enzyme modified cheese), cheese foods (which are produced by processing one or more kinds of natural or process cheese and have a cheese weight of 51% or higher in the product), butters, yogurts, creams, spreads, modified milk powders, and seasonings (to be used, for example, for snacks, dressings, and soups). Milks that are used as the main raw material for dairy products are ones from cows, sheep, goats, and others.

A modified enzyme or enzyme preparation of the present invention is added, for example, to a raw material or intermediate product during the course of producing the food product. This allows the enzyme to act on the milk fat present in the raw material or intermediate product, thereby leading to the release of fatty acids. The modified enzyme or enzyme preparation of the present invention can be added at various stages in the course of producing the dairy product. Amounts (concentrations) of enzyme to be used, temperature conditions, reaction time, and others may be determined through preliminary experiments.

EXAMPLES A. Generation of New Lipases

The inventors carried out the investigation described below, with aiming at the generation of new lipases.

1. Objectives and Investigation Strategy

The inventors made investigations, paying attention to:

(1) Aiming at acquiring a microbial lipase that provides a similar composition of released fatty acids to that provided by a calf sublingual gland derived lipase when the microbial lipase is allowed to act on cheese. In particular, attempts were made to change the fatty acid specificity from long-chain to short-chain fatty acids.

(2) Making the substrate pocket of an enzyme protein small, thereby to change the substrate specificity.

(3) Replacing an amino acid in the substrate pocket with a more bulky amino acid, thereby to making the substrate pocket smaller.

2. Methods (1) Selection of Mutation Sites

Amino acids that interact with substrates were selected based on the sequence of Candida cylindracea derived lipase LIP1 (its amino acid sequence including the signal peptide is represented in SEQ ID NO: 1, and the sequence of the gene encoding the amino acid sequence in SEQ ID NO: 20, and the amino acid sequence of the mature lipase without the signal peptide in SEQ ID NO: 2) and on the three dimensional structures deposited in public databases. Specifically, proline at position 261 (P261), leucine at position 319 (L319), and leucine at position 428 (L428) were selected. These amino acid residues correspond to P246, L304, and L413, respectively, in the literature by Schmitt et al. (Non Patent Document 1: J. Schmitt et al., Protein Engineering, vol. 15, no. 7, pp. 595-601, 2002).

At the same time, mutation sites were searched by computer analysis with taking note of the increase of the hydrophobicity in the pocket to improve the ability to synthesize esters. Serine at position 380 (S380) and glycine at position 429 (G429), which are neutral amino acids, were selected.

(2) Acquirement of DNA Sequences Encoding Mutated Amino Acid Sequences

A Pichia pastoris host expression system (Invitrogen, Pichia Expression Kit) was used. As a plasmid, pPIC3.5k was used. The gene for Candida cylindracea derived LIP1 that was used as a template was an LIP1-encoding sequence codon-optimized for Saccharomyces cerevisiae. Mutations were introduced by Inverse PCR method (TOYOBO, KOD-Plus-Mutagenesis Kit), thereby preparing genes encoding various variants with an amino acid substitution occurring at selected sites for mutation. A plasmid carrying a mutated LIP1 gene was transformed into E. coli strain DH5a. Subsequently, the plasmid carrying the mutated LIP1 gene was extracted from transformed E. coli cells.

(3) Acquirement of Transformants Expressing Mutated Amino Acid Sequences

The plasmid carrying the mutated LIP1 gene was transformed into Pichia pastoris strain GS115 (Invitrogen, Pichia Expression Kit). A resulting Pichia pastoris transformant was cultured and the enzyme (variant lipase) was collected form the cultured supernatant.

(4) Decomposition of Milk Fat using Variant Lipases

As a substrate, natural cheese (young Cheddar cheese) was used which was suspended and dispersed in phosphate buffer (pH 6.8) at a weight ratio of 1:1. The reaction was carried out under conditions at 50 ° C. for 16 hours. The amount of each variant lipase to be added was 0.1 mg protein per 1 g of cheese. After the reaction was completed, the released fatty acids in the cheese were extracted with diethyl ether and subjected to gas chromatography.

From the results of evaluation on more than ten variant lipases, it was found that several of the variant lipases gave a composition of the released fatty acids that, unlike that in the case of a wild-type lipase (FIG. 1), was similar to that in the case of a calf sublingual gland derived lipase (variant 1: L428N, variant 2: G429F, variant 3: G429M, and variant 4: G429I; FIG. 2). Accordingly, the inventors have succeeded in obtaining variant lipases that selectively release short-chain to medium-chain fatty acids (C₄ to C₈ fatty acids). When allowed to act on milk fat, these variant lipases work well on short-chain fatty acids (C₄ to C₆ fatty acids), and best on C₄ fatty acid. Among these variant lipases, variant 3 is remarkable in that it is more specific for short-chain fatty acids than the calf sublingual gland derived lipase. For comparison, the result for the variant L428F reported in the above-mentioned literature (which is referred to therein as L413F) is shown (FIG. 2, upper right panel). Variant L428F releases long-chain fatty acids in relatively large amounts. The amino acid sequences of these variants and the sequences of the genes encoding them (wherein codons characteristic of Candida yeasts are used so as to correspond to wild type lipase) are as follows:

<Variant 1>

Amino acid sequence: SEQ ID NO: 8

Gene sequence: SEQ ID NO: 12

<Variant 2>

Amino acid sequence: SEQ ID NO: 9

Gene sequence: SEQ ID NO: 13

<Variant 3>

Amino acid sequence: SEQ ID NO: 10

Gene sequence: SEQ ID NO: 14

<Variant 4>

Amino acid sequence: SEQ ID NO: 11

Gene sequence: SEQ ID NO: 15

B. Expression of a Variant Lipase in Various Hosts

(1) Expression of a Variant Lipase in Escherichia coli

A gene for a variant lipase (G429M) was inserted into a plasmid pET20b. The variant lipase was expressed using Escherichia coli Origami B (DE3) as a host. A resulting transformant was cultured under conditions at 15° C. for 40 hours to obtain bacterial cells. The bacterial cells were disrupted with a Bead Shocker, and lipase activity of the resultant extract was measured. For measuring the lipase activity for short-chain fatty acids, a Lipase Kit S (DS Biopharma Medical) was used. For measuring the lipase activity for long-chain fatty acids, a fat-digesting capacity LMAP method was used. The results revealed that the lipase activity of the cell extract was 1.85 u/mL when the Lipase Kit S was used and 0 u/mL when the LMAP method was used.

A gene for a variant lipase (G429M) was inserted into a plasmid pCold-TF. The variant lipase was expressed using Escherichia coli Origami B (DE3) as a host. A resulting transformant was cultured in LB medium under conditions at 15° C. for 40 hours to obtain bacterial cells. The bacterial cells were disrupted with a Bead Shocker, and lipase activity of the resultant extract was measured. The results revealed that the lipase activity of the cell extract was 3.95 u/mL when the Lipase Kit S was used and 0 u/mL when the LMAP method was used.

As mentioned above, a variant lipase (G429M) specific for short-chain fatty acids was able to be expressed.

(2) Expression of a Variant Lipase in a Yeast (Candida cylindracea) Strain

A variant lipase (G429M) was expressed using as a host a strain of Candida cylindracea that had been made auxotrophic by mutagenesis. A resulting transformant was cultured under conditions at 25° C. for 48 hours, and lipase activity of the cultured supernatant was measured. For measuring the lipase activity for short-chain fatty acids, an FCCIII method was used. For measuring the lipase activity for long-chain fatty acids, a fat-digesting capacity LMAP method was used. The results revealed that the lipase activity of the cultured supernatant of the Candida cylindracea strain in which the variant lipase (G429M) was allowed to be expressed was 470 u/mL when the FCIII 23 method was used and 155 u/mL when the LMAP method was used (a ratio of short-chain to long-chain fatty acids=3:1). For comparison, when a measurement was made of the lipase activity of the cultured supernatant of the parent host strain into which the variant lipase gene had been not introduced, the activity was 267 u/mL when the FCIII method was used and 599 u/mL when the LMAP method was used (a ratio of short-chain to long-chain fatty acids=2:5).

As mentioned above, a variant lipase (G429M) specific for short-chain fatty acids was able to be expressed.

(3) Expression of a variant lipase in a filamentous fungus (Aspergillus oryzae) strain A variant lipase (G429M) was expressed using as a host a strain of Aspergillus oryzae that had been made auxotrophic by mutagenesis and by means of using an amylase promoter. A resulting transformant was cultured under conditions at 30° C. for 76 hours, and lipase activity of the cultured supernatant was measured. For measuring the lipase activity for short-chain fatty acids, an FCCIII method was used. For measuring the lipase activity for long-chain fatty acids, a fat-digesting capacity LMAP method was used. The results revealed that the lipase activity of the cultured supernatant of the Aspergillus oryzae strain in which the variant lipase (G429M) was allowed to be expressed was 39 u/mL when the FCIII method was used and 0 u/mL when the LMAP method was used.

As mentioned above, a variant lipase (G429M) specific for short-chain fatty acids was able to be expressed.

(4) Expression of a Variant Lipase in a Bacillus subtilis Strain

Into a plasmid pHY300PLK was inserted a variant lipase (G429M) gene having a pullulanase promoter added thereto. The variant lipase was expressed using a Bacillus subtilis strain as a host. Lipase activity of the cultured medium of a resulting transformant was measured. For measuring the lipase activity for short-chain fatty acids, a Lipase Kit S (DS Biopharma Medical) was used. For measuring the lipase activity for long-chain fatty acids, a fat-digesting capacity LMAP method was used. The results revealed that the lipase activity of the cultured medium was 0.3 u/mL (and 0.1 u/mL for a control strain transformed with an empty vector) when the Lipase Kit S was used and 0 u/mL when the LMAP method was used.

As mentioned above, a variant lipase (G429M) specific for short-chain fatty acids was able to be expressed.

INDUSTRIAL APPLICABILITY

The modified lipase according to the present invention exhibits specificity for short-chain to medium-chain fatty acids. The modified lipase according to the present invention has a great deal of potential, in particular, in the production of dairy products having a cheese flavor, such as cheeses or cheese products.

The present invention should not be limited in any way to the description of the embodiments and examples of the above-described invention. The present invention also includes a variety of modified embodiments within the scope that one skilled in the art could easily arrive without departing from the description of the scope of claims. The contents of articles, published patent applications, patent publications, and others that are expressly provided are incorporated in their entire content by citation. 

1-16 (canceled)
 17. A modified lipase consisting of an amino acid sequence with a substitution made in the amino acid sequence of a lipase, wherein the substitution is: (1) a substitution of asparagine for an amino acid corresponding to the amino acid at position 428 in the amino acid sequence set forth in SEQ ID NO: 1; or (2) a substitution of phenylalanine, methionine, or isoleucine for an amino acid corresponding to the amino acid at position 429 in the amino acid sequence set forth in SEQ ID NO:1, wherein the amino acid sequence of the lipase is an amino acid sequence that is 90% or more identical to the amino acid sequence of SEQ ID NO: 2 and wherein the substitution is the substitution represented in (1), or wherein the amino acid sequence of the lipase is an amino acid sequence that is 90% or more identical to the amino acid sequence of SEQ ID NO: 2 and wherein the substitution is the substitution represented in (2).
 18. The modified lipase according to claim 17, wherein the amino acid sequence of the lipase is an amino acid sequence of SEQ ID No.
 2. 19. The modified lipase according to claim 17, consisting of the amino sequence set forth in SEQ ID No.
 10. 20. A gene encoding the modified lipase according to claim
 17. 21. The gene according to claim 20, comprising the polynucleotide sequence set forth in SEQ ID No.
 14. 22. A recombinant DNA comprising the gene according to claim
 20. 23. A microorganism carrying the recombinant DNA according to claim
 22. 24. The microorganism according to claim 23, wherein the host is Escherichia coli, Candida cylindracea, Aspergillus oryzae, Bacillus subtilis, or Pichia pastoris.
 25. An enzyme preparation comprising the modified lipase according to claim
 17. 26. A method for improving the flavor of a food product or food raw material, wherein the enzyme according to claim 17 is allowed to act on the food product or food raw material.
 27. A method for producing a food product, wherein the enzyme according to claim 17 is allowed to act on a food raw material or intermediate product.
 28. The method according to claim 26, wherein the food product is a dairy product.
 29. A flavor-improving agent that is allowed to act on a food product or food raw material, comprising the modified lipase according to claim
 17. 30. A food product or food raw material obtained by treatment with the enzyme according to claim
 17. 31. The method according to claim 27, wherein the food product is a dairy product.
 32. A flavor-improving agent that is allowed to act on a food product or food raw material, comprising the enzyme preparation according to claim
 25. 